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PMID: 8038380 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S.

A comparison of DMPC- and DLPE-based lipid bilayers.

Biophysical journal ·Vol. 66 ·No. 4 ·1994-04-00 ·Pages 1076-87

Damodaran KV, Merz KM

Abstract

A 250 ps molecular dynamics simulation of the dimyristoylphosphatidylcholine (DMPC)-based lipid bilayer, including explicit water molecules, is reported. The solvent environment of the head groups and other structural properties of the bilayer have been analyzed and compared with experimental results as well as our previous simulation of the dilauroylphosphatidylethanolamine (DLPE)-based bilayer. From this comparison we find that the solvent structure around the DMPC head group (clathrate shell) is significantly different than that around the DLPE head group (typical hydrogen bonding interactions). We have modeled the probable relationship between the different solvent environments around the R-N(CH3)3+ (DMPC) and R-NH3+ (DLPE) head groups and the different interlammelar distances in these systems by performing potential of mean force (PMF) simulations on two N(CH3)4+ and NH4+ ions in water. From the PMF simulations it appears that the differences in the hydration of the DMPC and DLPE head groups is not responsible for the differences in the hydration force observed for these systems. We also find that the orientational polarization of DLPE and DMPC is similar, which suggests that solvent polarization is not responsible for the differences in the hydration repulsion behavior observed in these systems. We also examined the order parameters for DMPC and found them to be in reasonable agreement with experiment. Given the different characteristics of the DLPE and DMPC head groups, we suggest an explanation of the differences in the interlammellar spacings of bilayers composed of these like-charged lipids. From our DLPE simulations we find that the R-NH3+ head groups can interact with the nonesterified oxygens of the phosphate group in an intraleaflet or an interleaflet manner. For the latter a "cross link" between two leaflets can be formed, which causes a stabilization of the interlamellar spacings at fairly short distances. Moreover, due to the strong intraleaflet interaction we find that the DLPE interface is relatively "flat" (as opposed to DMPC-based bilayers), which results in a surface that has regions of positive and negative charge that reside in the same plane along the bilayer normal. Based on this we propose that the DLPE bilayer interface can correlate itself with another DLPE interface by alignment of the regions of positive (or negative) charge on one leaflet with the opposite charges on the opposing leaflet.

MeSH Terms
Biophysical Phenomena Biophysics Computer Simulation Dimyristoylphosphatidylcholine/chemistry Electrochemistry Lipid Bilayers/chemistry Models, Chemical Phosphatidylethanolamines/chemistry Solvents Thermodynamics
Chemicals
Lipid Bilayers Phosphatidylethanolamines Solvents 1,2-dilauroylphosphatidylethanolamine Dimyristoylphosphatidylcholine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Damodaran K V
Department of Chemistry, Pennsylvania State University, University Park 16802.
Merz K M
References (17)
17 references, click to expand
  1. Structure of a fluid dioleoylphosphatidylcholine bilayer determined by joint refinement of x-ray and neutron diffraction data. III. Complete structure.
    Biophys J. 1992 Feb;61(2):434-47 PMID: 1547331
  2. Structure of a fluid dioleoylphosphatidylcholine bilayer determined by joint refinement of x-ray and neutron diffraction data. II. Distribution and packing of terminal methyl groups.
    Biophys J. 1992 Feb;61(2):428-33 PMID: 1547330
  3. Contributions of hydration and steric (entropic) pressures to the interactions between phosphatidylcholine bilayers: experiments with the subgel phase.
    Biochemistry. 1993 Aug 17;32(32):8374-84 PMID: 8347634
  4. The dynamic structure of fatty acyl chains in a phospholipid bilayer measured by deuterium magnetic resonance.
    Biochemistry. 1974 Nov 5;13(23):4839-45 PMID: 4371820
  5. Calcium, tropomyosin, and actomyosin as controls of calcium binding by troponin.
    Recent Adv Stud Cardiac Struct Metab. 1975;8:233-40 PMID: 1215638
  6. Deuterium magnetic resonance: theory and application to lipid membranes.
    Q Rev Biophys. 1977 Aug;10(3):353-418 PMID: 335428
  7. Temperature and compositional dependence of the structure of hydrated dimyristoyl lecithin.
    J Biol Chem. 1979 Jul 10;254(13):6068-78 PMID: 447695
  8. The molecular structure of lecithin dihydrate.
    Nature. 1979 Oct 11;281(5731):499-501 PMID: 492310
  9. Neutron diffraction studies on phosphatidylcholine model membranes. I. Head group conformation.
    J Mol Biol. 1979 Nov 15;134(4):673-91 PMID: 537074
  10. Preferred conformation and molecular packing of phosphatidylethanolamine and phosphatidylcholine.
    Biochim Biophys Acta. 1981 Jun 16;650(1):21-51 PMID: 7020761
  11. Hydration force and bilayer deformation: a reevaluation.
    Biochemistry. 1986 Jul 15;25(14):4058-66 PMID: 2427111
  12. Hydration and the lamellar to hexagonal II phase transition of phosphatidylethanolamine.
    Biochemistry. 1986 Nov 18;25(23):7518-22 PMID: 3801431
  13. Lipid chains and cholesterol in model membranes: a Monte Carlo Study.
    Biochemistry. 1989 May 2;28(9):3687-91 PMID: 2751989
  14. Magnitude of the solvation pressure depends on dipole potential.
    Proc Natl Acad Sci U S A. 1989 Dec;86(23):9263-7 PMID: 2594765
  15. Range of the solvation pressure between lipid membranes: dependence on the packing density of solvent molecules.
    Biochemistry. 1989 Sep 19;28(19):7904-12 PMID: 2611220
  16. Model for the structure of the lipid bilayer.
    Proc Natl Acad Sci U S A. 1991 Feb 1;88(3):892-6 PMID: 1992480
  17. Structure and dynamics of the dilauroylphosphatidylethanolamine lipid bilayer.
    Biochemistry. 1992 Aug 25;31(33):7656-64 PMID: 1510951
Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
1994-04-00
Pages
1076-87
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1275815
Subset
IM
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